Names | |
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Preferred IUPAC name
(3R)-5-Methoxy-1′-methylspiro[indole-3,3′-pyrrolidin]-2(1H)-one | |
Identifiers | |
3D model (
JSmol)
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ChemSpider | |
PubChem
CID
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UNII | |
CompTox Dashboard (
EPA)
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Properties | |
C13H16N2O2 | |
Molar mass | 232.283 g·mol−1 |
Melting point | 125 to 126 °C (257 to 259 °F; 398 to 399 K) |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Horsfiline is an oxindole alkaloid found in the plant Horsfieldia superba, [1] which is used in traditional herbal medicine. It has analgesic effects[ medical citation needed] and has been the subject of research both to produce it synthetically by convenient routes [2] [3] [4] [5] [6] [7] [8] and to develop analogues and derivatives which may have improved analgesic effects. [9] [10]
It is a member of the spiroindolone class. Elacomine has a similar chemical structure.
Names | |
---|---|
Preferred IUPAC name
(3R)-5-Methoxy-1′-methylspiro[indole-3,3′-pyrrolidin]-2(1H)-one | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C13H16N2O2 | |
Molar mass | 232.283 g·mol−1 |
Melting point | 125 to 126 °C (257 to 259 °F; 398 to 399 K) |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Horsfiline is an oxindole alkaloid found in the plant Horsfieldia superba, [1] which is used in traditional herbal medicine. It has analgesic effects[ medical citation needed] and has been the subject of research both to produce it synthetically by convenient routes [2] [3] [4] [5] [6] [7] [8] and to develop analogues and derivatives which may have improved analgesic effects. [9] [10]
It is a member of the spiroindolone class. Elacomine has a similar chemical structure.